Medline Convenience Kits Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Medline Industries, LP is recalling 49,654 convenience kits nationwide because they contain a recalled lot of MASTISOL Liquid Adhesive with tubing that may crack during use.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 2, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
Medline Industries, LP initiated a voluntary recall of various convenience kits containing Ferndale Laboratories MASTISOL Liquid Adhesive. The butyrate tubing in the adhesive may crack during actuation, rendering the product unusable.
Which Products Are Affected
The recall covers 49,654 kits distributed nationwide in the United States (OUS distribution pending). Affected products include numerous Medline convenience kits such as ACD (DYNJ904999J), ACDF (DYNJ907336B, DYNJ910821A), ACL (DYNJ911996), and many others across orthopedic, spine, arthroscopy, and other surgical packs. Specific UDI-DI numbers and lot codes are detailed in FDA recall Z-2436-2026. Classification: Class II.
What You Should Do
Consumers and facilities should check inventory for the listed products and lots and follow instructions provided by Medline Industries, LP.
Why This Matters
The defect affects the usability of the adhesive component in surgical kits distributed across the United States.
Source
FDA Enforcement Report, recall number Z-2436-2026, initiated April 27, 2026.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,095 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 2, 2026.
Frequently Asked Questions
Common questions about this FDA recall.